Palindrome resolution and recombination in the mammalian germ line. - Wikidata - wikimedia - TriplyDB

Palindrome resolution and recombination in the mammalian germ line.

Palindrome resolution and recombination in the mammalian germ line.

http://www.wikidata.org/entity/Q36572432

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Tandemly arrayed genes in vertebrate genomes Evidence for active maintenance of inverted repeat structures identified by a comparative genomic approach Mechanisms of gene duplication and amplification Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual.Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure Genomic disorders on 22q11 Non-B DB: a database of predicted non-B DNA-forming motifs in mammalian genomes New approaches to the analysis of palindromic sequences from the human genome: evolution and polymorphism of an intronic site at the NF1 locus Chromosomal translocations and palindromic AT-rich repeats Unusually long palindromes are abundant in mitochondrial control regions of insects and nematodes NMR study of a heterochiral DNA hairpin:impact of L-enantiomery in the loop Molecular and Functional Characterization of a Cohort of Spanish Patients with Ataxia-Telangiectasia Polymorphic DAZ gene family in polymorphic structure of AZFc locus: Artwork or functional for human spermatogenesis?Identification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrhea Genomic rearrangements at the IGHMBP2 gene locus in two patients with SMARD1 DNA secondary structure at chromosomal fragile sites in human disease.A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2.DNA hairpin opening mediated by the RAG1 and RAG2 proteins.Palindrome-mediated chromosomal translocations in humans.Evolution of immunoglobulin and T-cell receptor gene assembly.DNA-directed mutations. Leading and lagging strand specificity.The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats.The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation.Parental origin and timing of de novo Robertsonian translocation formation.The distribution of inverted repeat sequences in the Saccharomyces cerevisiae genome.AT-rich palindromes mediate the constitutional t(11;22) translocation.DNA polymerase stalling, sister chromatid recombination and the BRCA genes.Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).High levels of sequence polymorphism and linkage disequilibrium at the telomere of 12q: implications for telomere biology and human evolution.Segmental duplications and gene conversion: Human luteinizing hormone/chorionic gonadotropin beta gene cluster.Chromosome instability as a result of double-strand breaks near telomeres in mouse embryonic stem cells Human meiotic recombination products revealed by sequencing a hotspot for homologous strand exchange in multiple HNPP deletion patients Molecular characterization of transgene integration by next-generation sequencing in transgenic cattle.Direct and inverted repeats elicit genetic instability by both exploiting and eluding DNA double-strand break repair systems in mycobacteria.Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability A novel recombination pathway initiated by the Mre11/Rad50/Nbs1 complex eliminates palindromes during meiosis in Schizosaccharomyces pombe.Evaluation of the Tg.AC transgenic mouse assay for testing the human carcinogenic potential of pharmaceuticals--practical pointers, mechanistic clues, and new questions.Factors affecting inverted repeat stimulation of recombination and deletion in Saccharomyces cerevisiae Long inverted repeats are an at-risk motif for recombination in mammalian cells.

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P2860

Palindrome resolution and recombination in the mammalian germ line.

http://www.wikidata.org/entity/Q36572432

description

1997 nî lūn-bûn

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1997年論文

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1997年论文

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1997年论文

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1997年论文

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name

Palindrome resolution and recombination in the mammalian germ line.

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Palindrome resolution and recombination in the mammalian germ line.

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type

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Palindrome resolution and recombination in the mammalian germ line.

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Palindrome resolution and recombination in the mammalian germ line.

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prefLabel

Palindrome resolution and recombination in the mammalian germ line.

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Palindrome resolution and recombination in the mammalian germ line.

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Palindrome resolution and recombination in the mammalian germ line.

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Akgün E

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P2860

Isolation and characterization of the human MRE11 homologue

Human Rad50 is physically associated with human Mre11: identification of a conserved multiprotein complex implicated in recombinational DNA repair

Chromosomal double-strand break repair in Ku80-deficient cells

Interaction of Mre11 and Rad50: two proteins required for DNA repair and meiosis-specific double-strand break formation in Saccharomyces cerevisiae.

The mechanism of V(D)J joining: lessons from molecular, immunological, and comparative analyses

The double-strand-break repair model for recombination

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

Trinucleotide repeats that expand in human disease form hairpin structures in vitro

Sister chromatid fusion initiates amplification of the dihydrofolate reductase gene in Chinese hamster cells.

Co-amplified markers alternate in megabase long chromosomal inverted repeats and cluster independently in interphase nuclei at early steps of mammalian gene amplification

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